Suppliers / Anlon Healthcare

Anlon Healthcare

India 43 employees Updated 9 July 2026

Anlon Healthcare is an API manufacturer based in India. It holds one valid CEP. Its GMP standing is certified by CDSCO (India). Customs aggregates show $13K of exports covering 3 molecules to 3 destinations in 2025.

0
active US DMFs
1
valid CEPs
2
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Gondal, India Not on file
pipaliya sadak rajkot, India Not on file

What they file, and where

Molecule Regulators Docs
Ketoprofen EDQM 1

Also appears on these molecule pages

Ketoprofen API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $434K 4
2025 Not reported $13K 3
2024 Not reported $908K 6
2023 Not reported $403K 4

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Anlon Healthcare

Does Anlon Healthcare hold a US DMF or a CEP?
Anlon Healthcare holds 1 valid CEP. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Anlon Healthcare manufacture?
2 registered sites are on record, in India (Gondal and Pipaliya Sadak Rajkot). Every site is listed on this page with the register it came from.
What does Anlon Healthcare make?
1 molecule is on record against Anlon Healthcare, including Ketoprofen. Each links through to that molecule's full manufacturer list.
Which regulators recognise Anlon Healthcare's GMP?
Current GMP certificates are on record from CDSCO (India). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Comparable suppliers

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts